반응 #323040
ord-fb9827c73e1245b394d8bb3d31b4abe0
반응 방정식
용매
반응 조건
온도
4°CELSIUS
상세 조건
See reaction.notes.procedure_details.
후처리
- 1workup.DISSOLUTIONis dissolved
- 2기타the crystallised solid is separated by filtration
- 3세척washed with ethanol (2×10 cc)
- 4기타dried at 45° C. under reduced pressure (0.067 kPa)
실험 절차
The procedure is similar to that described in Example 1, but starting with 2-furancarboxylic acid (8.95 g), N,N'-carbonyldiimidazole (12.8 g) and 2-amino-7-methoxy-1,8-naphthyridine (10.5 g). The product produced by precipitation in water (15.5 g; m.p. 199° C.) is dissolved in boiling ethanol (500 cc). After 2 hours' cooling at 4° C., the crystallised solid is separated by filtration, washed with ethanol (2×10 cc) and dried at 45° C. under reduced pressure (0.067 kPa). N-(7-Methoxy-1,8-naphthyridin-2-yl)-2-furancarboxamide (13.5 g) is produced, m.p. 201° C.